| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:142854990-142855184 | Common:3; Rare:56 | ||||
| chr7:143288155-143288442 | Common:1; Rare:106 | ||||
| chr7:143361051-143361743 | Common:4; Rare:103 | ||||
| chr7:143361774-143361979 | Rare:57 | ||||
| chr7:143362101-143362354 | Rare:35 | ||||
| chr7:143362691-143362949 | Common:1; Rare:73 | ||||
| chr7:143380931-143381323 | Common:1; Rare:119 | ||||
| chr7:143882753-143883003 | Rare:63 | ||||
| chr7:143885232-143885487 | Common:1; Rare:80 | ||||
| chr7:143902089-143902283 | Common:7; Rare:64 | ||||
| chr7:144835979-144836115 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr7:146115724-146115873 | Rare:33 | ||||
| chr7:146116127-146116483 | Rare:88; Clinvar:1 | ||||
| chr7:148339064-148339633 | Common:10; Rare:129 | ||||
| chr7:148698122-148698340 | Common:4; Rare:58 |